FDA Food recall F-0729-2022
MidNite Tablet (Melatonin 1.5 mg) supplement, ULTRAtab Laboratories, Inc., Highland, NY
- FDA Food
- Class II
- terminated
- Published 2022-02-16
On 2022-02-16 the FDA classified a Class II recall of MidNite Tablet (Melatonin 1.5 mg) supplement, ULTRAtab Laboratories, Inc., Highland, NY by Ultratab Laboratories, citing cGMP Deviations.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-0729-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-10-06 |
| Published | 2022-02-16 |
| Last updated | 2026-09-13 11:50 UTC |
| Company | Ultratab Laboratories |
| Distribution | FL, NY |
Product
MidNite Tablet (Melatonin 1.5 mg) supplement, ULTRAtab Laboratories, Inc., Highland, NY
Reason
cGMP Deviations
Identifiers
| code_info | Product Codes: M978 Bulk Lots: 18J069, 18J070, 18J071, 18M072, 18L124, 18L125, 18L126, 19C037, 19C038, 19C039, 19C040,1…Product Codes: M978 Bulk Lots: 18J069, 18J070, 18J071, 18M072, 18L124, 18L125, 18L126, 19C037, 19C038, 19C039, 19C040,19D029, 19D030, 19D031, 19G047, 19G048, 19G049, 19G050 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:50 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0729-2022%22
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